Ascorbate inhibition of angiogenesis in aortic rings ex vivo and subcutaneous Matrigel plugs in vivo.

Nina A Mikirova, Joseph J Casciari, Neil H Riordan
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引用次数: 38

Abstract

Background: Angiogenesis is critical to tumor growth and is therefore a potential target for cancer therapy. As many current inhibitors of angiogenesis exhibit host toxicity, natural alternatives are needed. At millimolar concentrations, ascorbate (vitamin C) inhibits migration and tubule formation by mature endothelial cells and endothelial progenitors. In the present study, we examined the effects of ascorbate, at levels relevant during intravenous infusion therapy, on angiogenesis using an ex vivo an in vivo assay.

Methods: Two assays were used to evaluate effect of high-doses ascorbic acid on angiogenesis: ex vivo rat aortic ring explant assay in Matrigel matrices and in vivo Matrigel plug assay. In aortic rings, we quantified microvessel growth, branching and vessel regression under different treatment conditions. In murine angiogenesis assay, male C57 mice 6-8 weeks old were treated by high-dose ascorbic acid and the number of microvessels was analyzed by histological method. To characterize the population of cells that formed capillary network and microvessels, the sections were stained by CD34 and CD31 antibodies.

Results: Results show that sprouting of endothelial tubules from aortic rings was reduced in a concentration-dependent fashion by ascorbate: while controls roughly tripled sprout densities during the study, ascorbate (1 mg/mL, 5.5 mM) actually reduced sprout density. In vivo, the ability of mice to vascularize subcutaneously implanted Matrigel plug was diminished if the mice were treated with 430 mg/kg vitamin C: numbers of vessels, and vessel densities, in plugs from treated mice were roughly 30% less than those in plugs from untreated mice.

Conclusions: We conclude that the inhibition of angiogenesis by ascorbate suggested in vitro is confirmed in vivo, and that angiogenesis inhibition may be one mechanism by which intravenous ascorbate therapy shows efficacy in animal experiments and clinical case studies.

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抗坏血酸抑制体外主动脉环血管生成和体内皮下基质塞。
背景:血管生成对肿瘤生长至关重要,因此是癌症治疗的潜在靶点。由于目前许多血管生成抑制剂表现出宿主毒性,因此需要天然的替代品。在毫摩尔浓度下,抗坏血酸(维生素C)抑制成熟内皮细胞和内皮祖细胞的迁移和小管形成。在目前的研究中,我们通过体外和体内实验检测了抗坏血酸在静脉输注治疗期间相关水平对血管生成的影响。方法:采用大剂量抗坏血酸对血管生成的影响:体外大鼠主动脉环基质外植体实验和体内基质塞实验。在主动脉环中,我们量化了不同处理条件下微血管的生长、分支和血管退化。在小鼠血管生成实验中,用大剂量抗坏血酸处理6-8周龄雄性C57小鼠,用组织学方法分析微血管数量。为了表征形成毛细血管网络和微血管的细胞群,切片用CD34和CD31抗体染色。结果:结果显示,抗坏血酸降低了主动脉环内皮小管的发芽,其浓度依赖于抗坏血酸:在研究期间,抗坏血酸(1mg /mL, 5.5 mM)实际上降低了发芽密度,而对照组大约增加了三倍的发芽密度。在体内,如果小鼠接受430 mg/kg维生素C治疗,小鼠皮下植入的Matrigel塞的血管化能力就会减弱:治疗小鼠塞的血管数量和血管密度比未治疗小鼠塞的血管数量和血管密度大约少30%。结论:我们认为抗坏血酸在体外对血管生成的抑制作用在体内得到了证实,血管生成抑制可能是静脉注射抗坏血酸治疗在动物实验和临床病例研究中显示疗效的机制之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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